CN112795405B - System for coal gas circulation coal pyrolysis coupling chemical chain gasification coproduction oil gas - Google Patents
System for coal gas circulation coal pyrolysis coupling chemical chain gasification coproduction oil gas Download PDFInfo
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- 238000000197 pyrolysis Methods 0.000 title claims abstract description 114
- 239000003245 coal Substances 0.000 title claims abstract description 110
- 238000002309 gasification Methods 0.000 title claims abstract description 104
- 239000000126 substance Substances 0.000 title claims abstract description 41
- 239000003034 coal gas Substances 0.000 title claims abstract description 28
- 238000010168 coupling process Methods 0.000 title claims abstract description 17
- 230000008878 coupling Effects 0.000 title claims abstract description 14
- 238000005859 coupling reaction Methods 0.000 title claims abstract description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 85
- 239000001301 oxygen Substances 0.000 claims abstract description 85
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 85
- 239000007789 gas Substances 0.000 claims abstract description 76
- 238000006243 chemical reaction Methods 0.000 claims abstract description 72
- 230000008929 regeneration Effects 0.000 claims abstract description 47
- 238000011069 regeneration method Methods 0.000 claims abstract description 47
- 239000007787 solid Substances 0.000 claims abstract description 31
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 29
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 22
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 22
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 20
- 238000007885 magnetic separation Methods 0.000 claims abstract description 19
- 239000002994 raw material Substances 0.000 claims abstract description 9
- 239000013589 supplement Substances 0.000 claims abstract description 4
- 230000003197 catalytic effect Effects 0.000 claims abstract description 3
- 238000000926 separation method Methods 0.000 claims description 43
- 239000000428 dust Substances 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 238000001035 drying Methods 0.000 claims description 17
- 238000002485 combustion reaction Methods 0.000 claims description 15
- 239000002245 particle Substances 0.000 claims description 15
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 14
- 239000011335 coal coke Substances 0.000 claims description 14
- 239000003546 flue gas Substances 0.000 claims description 14
- 239000000047 product Substances 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 12
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- 238000007254 oxidation reaction Methods 0.000 claims description 11
- 239000002351 wastewater Substances 0.000 claims description 9
- 238000003860 storage Methods 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 238000010521 absorption reaction Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000000571 coke Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 238000011084 recovery Methods 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 4
- 238000004523 catalytic cracking Methods 0.000 claims description 4
- 230000002950 deficient Effects 0.000 claims description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000012071 phase Substances 0.000 claims description 4
- 238000010298 pulverizing process Methods 0.000 claims description 4
- 239000007790 solid phase Substances 0.000 claims description 4
- 230000001105 regulatory effect Effects 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 239000002912 waste gas Substances 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims 2
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- 238000004364 calculation method Methods 0.000 description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
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- 238000003912 environmental pollution Methods 0.000 description 2
- 239000002918 waste heat Substances 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 208000036828 Device occlusion Diseases 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
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- VTVVPPOHYJJIJR-UHFFFAOYSA-N carbon dioxide;hydrate Chemical compound O.O=C=O VTVVPPOHYJJIJR-UHFFFAOYSA-N 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 239000007805 chemical reaction reactant Substances 0.000 description 1
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- 230000005484 gravity Effects 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000006148 magnetic separator Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
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- 239000006163 transport media Substances 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/02—Fixed-bed gasification of lump fuel
- C10J3/20—Apparatus; Plants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B53/00—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/82—Gas withdrawal means
- C10J3/84—Gas withdrawal means with means for removing dust or tar from the gas
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
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- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Abstract
The invention provides a system for co-producing oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification. The chemical chain gasification unit takes pyrolytic semicoke as a raw material and oxygen carrier lattice oxygen as an oxygen source, and synthesis gas and a reduced oxygen carrier are obtained by reaction; the pyrolysis unit adopts a fluidized bed as a pyrolysis reactor, a gas-solid two-phase heat carrier as a heat source, pyrolysis gas and high-temperature gasification synthesis gas exchange heat and then are used as a gas heat carrier to circulate, and a reduced oxygen carrier with a certain catalytic action is used as a solid heat carrier to supplement heat; the reduced oxygen carrier separated by magnetic separation enters an air regeneration reactor and is regenerated into an oxidized state. The invention takes coal as raw material, and prepares tar and synthesis gas simultaneously by coupling coal pyrolysis and chemical chain gasification through the oxygen carrying, catalyzing and heat carrying capacities of the oxygen carrier, thereby realizing the gradient utilization of coal and having the advantages of high carbon conversion rate, low system energy consumption, environmental protection and the like.
Description
Technical Field
The invention relates to a coal step conversion and tar and synthesis gas co-production process system, which can be used in the field of clean and efficient utilization of coal, and particularly relates to a coal dry distillation, tar catalytic reforming and chemical chain co-production oil gas system.
Background
As the most abundant fossil raw materials in our country, the method has a leading position in the primary energy consumption structure of our country. However, in the development and utilization process of coal resources, China still has a series of problems of environmental pollution, low utilization efficiency and the like. How to solve the problem of sustainable development of coal resources is urgent. Aiming at the current utilization situation of coal energy in China, the key of sustainable development of the structure of the Chinese energy industry is to improve the traditional utilization mode of the coal resource, improve the utilization efficiency, reduce the environmental pollution and realize the clean utilization and low-carbon emission of the coal resource.
The main modes for efficiently and cleanly utilizing resources comprise coal liquefaction, coal pyrolysis and coal gasification. Coal gasification is one of core technologies for realizing efficient and clean utilization of coal, and the produced synthesis gas is widely applied to the aspects of natural gas for urban life, fuel gas for industrial production, synthesis gas, reducing gas and the like, and is a core process of the modern coal chemical industry. However, the traditional coal gasification process has the problems of high carbon emission intensity, high process energy consumption and the like, and the coal pyrolysis and gasification are carried out in the same reactor, and each sub-reaction has interaction, so that the targeted selective regulation and control of the synthesis gas in the conversion process are hindered.
The chemical process replaces the traditional oxygen-rich gasifying agent with lattice oxygen of oxygen carrier and participates in the gasifying reaction to prepare the synthetic gas. Compared with the traditional coal gasification, the air separation device is completely replaced, and the energy consumption and the cost are obviously reduced; the oxygen carrier releases a large amount of reaction heat in the regeneration reactor, and the heat is brought into the gasification reactor by the oxygen carrier for coal gasification, so that the self-heating balance is realized; the participation of the oxygen carrier can inhibit NO in the coal gasification processX、SOXThe generation is more efficient and environment-friendly. However, the research aiming at the chemical chain gasification technology at present is lack of the joint development of other emerging clean energy technologies, the development of the clean coal technology is promoted by fully playing the role of '1 +1 > 2', and a great thrust effect is played for the development and utilization of the coal resources in China.
The coal pyrolysis coupled chemical chain gasification process fully considers the advantages and the defects of the single coal chemical technology, and realizes the advantage complementation. The main points are as follows: 1) compared with single coal pyrolysis, the coupling process not only extracts tar resources with high added value in lignite in the coal pyrolysis stage, improves coal conversion and utilization economy, but also considers the problem of semicoke utilization neglected in the traditional coal pyrolysis, takes high-quality semicoke with high heat value and high carbon content as a raw material for chemical chain gasification, and fully realizes maximization of coal resource element utilization; 2) compared with the coal single chemical-looping gasification, the coupling process can solve the problems of device blockage, oxygen carrier coking and the like caused by tar generated in the coal chemical-looping gasification process, and in the coal gas circulation process, the coal pyrolysis phenolic wastewater is used as a water gas shift reaction reactant, so that the tar quality can be improved, and near zero emission of the coal pyrolysis wastewater is realized; 3) from the aspect of overall energy utilization efficiency, the coupling process fully considers the energy utilization problems of pyrolysis high-temperature semicoke and gasification high-temperature synthesis gas, not only realizes the step conversion of coal resources, but also realizes the high-efficiency energy transfer by utilizing the temperature gradient of each reaction unit and the cyclic heat exchange of the oxygen carrier and the gas, and improves the energy utilization efficiency.
Disclosure of Invention
The invention aims to solve the problems of the existing coal pyrolysis and coal gasification technologies, and provides a system and a method for co-producing oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification.
The technical scheme of the invention is as follows:
a system for co-producing oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification comprises a raw coal pretreatment system, a coal pyrolysis system, a coal coke chemical chain gasification system and an oxygen carrier air regeneration system;
the raw coal pretreatment system comprises a raw coal bunker 1, a crushing and pulverizing device 2, a drying reactor 3, a gas-liquid separation tank 12 and CO2An absorption tower 13; raw coal in a raw coal bunker 1 is made into pulverized coal with the particle size of 0.05-0.1 mm through a crushing and pulverizing device 2, and is mixed and dried in a drying reactor 3 with high-temperature dedusting flue gas generated by a carbon residue combustion reactor 17 in a coke chemical chain gasification system; the waste water is separated from the water-containing waste gas generated in the drying reactor 3 by the gas-liquid separation tank 12, and then is treated by CO2Absorption tower 13 for separating CO2And N2Taking the dried coal sample as a raw material to enter a coal pyrolysis system;
the coal pyrolysis system comprises a feeding hopper 4, a slide valve feeding device 5, a pyrolysis reactor 6, a two-stage cyclone separator 22, a first cyclone dust collector A7-1, a condenser 8, an oil storage tank 9, an electric oil catcher 21, a first magnetic separation device A10-1 and a first heat exchanger A11-1; raw coal pretreated by the drying reactor 3 sequentially passes through a first feeding hopper A4-1 and a first slide valve feeding device A5-1, and sequentially passes through a second feeding hopper B4-24-24 and a reduced state oxygen carrier fed by a second slide valve feeding device B5-2, and then enters a pyrolysis reactor 6 with a two-stage cyclone separator 22 arranged inside, and semi-coke, tar and pyrolysis coal gas are obtained in the pyrolysis reactor 6; pyrolysis gas and tar mixture enter a first cyclone dust collector A7-1 from the upper outlet end of the pyrolysis reactor 6, and after dust removal treatment is carried out on the pyrolysis gas and tar mixture by the first cyclone dust collector A7-1, the tar enters a condenser 8, is condensed by the condenser 8 and is stored in an oil storage tank 9; an electric oil catcher 21 is arranged at the outlet of the oil storage tank 9 and used for recovering tar carried by gas; the pyrolysis coal gas after tar recovery and the high-temperature gasification synthesis gas generated by the coal coke chemical-looping gasification system exchange heat in a first heat exchanger A11-1 and then enter a pyrolysis reactor 6 as a gas heat carrier; the semicoke and the reduced-state oxygen carrier enter a first magnetic separation device A10-1 through the lower outlet end of the pyrolysis reactor 6, are separated by the first magnetic separation device A10-1, the semicoke is used as a raw material of a coal coke chemical chain gasification system, and the reduced-state oxygen carrier is regenerated in an air regeneration reactor 18;
the pyrolysis reactor 6 is an internal heating fluidized bed reactor, the reaction is divided into an upper section and a lower section, the lower section is a dense-phase region, the upper section is a dilute-phase region, a two-stage cyclone separator 22 is arranged in the pyrolysis reactor, and the lower end of the cyclone separator 22 is provided with a wing valve; the temperature of the pyrolysis reactor 6 is 500-600 ℃, and the oxygen carrier from the gasification reactor is Fe3O4The catalytic cracking of tar is promoted by the continuous release and supplement of lattice oxygen; after external heat exchange, the pyrolysis gas at 650-750 ℃ is used as a gas heat carrier and returns to the pyrolysis reactor 6 to provide heat for the pyrolysis reaction; the 550-650 ℃ reduced oxygen carrier with catalytic action enters the pyrolysis reactor 6 through a slide valve device together with the coal sample; the temperature of the condenser 8 is 120-150 ℃, the quality of tar is improved, and meanwhile, the phenol-containing wastewater provides a hydrogen source for the light tar.
In the coal pyrolysis system, the following reactions mainly occur:
drying and slight pyrolysis of raw coal
Raw coal → dry coal + waste water, endothermic reaction.
Coal pyrolysis
Coal → semicoke + tar + pyrolysis gas CO, CO2、H2、H2O、CH4Etc., endothermic reaction.
Catalytic reforming of tar
Heavy tar + -O- → light tar, light aromatic hydrocarbons, phenol, cresol, etc., endothermic reaction.
The coal coke chemical looping gasification system comprises a jet device 14, a gasification reactor 15, a first cyclone separator A16-1, a second magnetic separation device B10-2, a carbon residue combustion reactor 17 and a second cyclone dust collector B7-2; the semicoke fed through the first jet device A14-1 and the oxidation state oxygen carrier fed through the second jet device B14-2 enter the gasification reactor 15 together, and the gasifying agent CO is supplemented2And H2O, carrying out gasification reaction to prepare synthesis gas; the gasification product enters a first cyclone separator A16-1 from an outlet at the top end of the gasification reactor 15, and the synthesis gas and the solid phase residue are separated by the first cyclone separator A16-1; exchanging heat between the high-temperature synthesis gas and low-temperature pyrolysis coal gas generated by a coal pyrolysis system in a first heat exchanger A11-1, and taking the synthesis gas after heat recovery as a product to be stored in a tank area; the solid phase residue is separated into a reduction state oxygen carrier and unreacted carbon by a second magnetic separation device B10-2, the unreacted carbon is fully combusted in a combustion reactor 17 to generate high-temperature flue gas, and the dusty flue gas enters a drying reactor 3 after being subjected to dust removal treatment in a second cyclone dust collector B7-2 to provide heat for drying raw coal; returning part of the reduced oxygen carrier to the pyrolysis reactor 6 to be used as a solid heat carrier and a catalyst, and oxidizing the rest of the reduced oxygen carrier to an air regeneration reactor 18 to be a high valence state oxygen carrier;
the gasification reactor 15 is a vertical cyclone furnace, the flow pattern is a fast fluidized bed/pneumatic conveying bed flow pattern, and the fluidizing medium is high-temperature CO2And water vapor; the temperature of the gasification reactor 15 is 800-900 ℃, and the temperature of the gasification reactor 10 from the air regeneration reactor 1800~1100℃Fe2O3The oxygen carrier is used as a solid heat carrier to provide heat for gasification reaction, so that the energy utilization efficiency is improved; the gasification reactor 15 is fed in a manner of opposed feeding such that the semicoke and Fe are opposed2O3The particles are mixed more uniformly and the collision reaction is more violent; the two-stage gasification reactor 15 has a fast reaction stage at the lower stage, mainly generates chemical chain gasification reaction between coal coke particles and oxygen carrier particles, the carbon conversion rate is about 0.6, the hydrogen production reaction between Fe/FeO and water vapor at the upper stage, and the oxygen carrier and residual carbon perform deep reaction at the same time, the carbon conversion rate is about 0.9, so as to realize H in synthesis gas2the/CO is adjustable; the gasification reactor 15 is fed in a manner of opposed feeding such that the semicoke and Fe are opposed2O3The mixing is more uniform, and the collision reaction is more violent; the carbon content of ash is 6-10%, the temperature of a carbon residue combustion reactor is 500-600 ℃, and the step conversion and comprehensive utilization of coal are realized through high-temperature flue gas heat exchange;
the oxygen carrier particles are Fe2O3Meanwhile, other transition metal elements such as Ni, Cu, Co, Mn and the like can be used for substitution or doping.
The separation device mainly comprises gas-solid separation and solid-solid separation, wherein the gas-solid separation device comprises a cyclone separator and a cyclone dust collector, and the separation efficiency is 95-99%; the solid-solid separation adopts a magnetic separation mode, and the separation efficiency is 95-99%.
In a coal coke chemical looping gasification system, the following reactions mainly occur:
coke particle reduction
C+CO2→2CO,ΔH298=+172kJ/mol;
C+H2O→CO+H2,ΔH298=+131kJ/mol;
C+Fe2O3→CO+2FeO,ΔH298=+178kJ/mol。
Deep side reaction of gasification products
CO+H2O→CO2+H2,ΔH298=-41kJ/mol;
CO+FeO→CO2+Fe,ΔH298=-16kJ/mol;
4H2+CO2→CH4+2H2O,ΔH298=-164kJ/mol;
H2+FeO→Fe+H2O,ΔH298=-18kJ/mol;
CH4+H2O→CO+3H2,ΔH298=+219kJ/mol;
CH4+CO2→2CO+2H2,ΔH298=+247kJ/mol。
Oxygen carrier hydrogen production reaction
4H2O+3Fe→Fe3O4+4H2,ΔH298=-148kJ/mol。
The oxygen carrier air regeneration system comprises a mixer 20, an air regeneration reactor 18, a spiral tube type heat exchanger 19, a second cyclone separator B16-2 and a second heat exchanger B11-2; the reduced oxygen carrier of the coal pyrolysis system and the coal coke chemical looping gasification system enters an air regeneration reactor 18 of an external spiral tube type heat exchanger 19 together with hot air through a mixer 20 to carry out oxidation regeneration reaction, so as to obtain a high-order oxidation state oxygen carrier and oxygen-deficient air; the oxygen carrier in the oxidation state and the oxygen-deficient air are separated in a second cyclone separator B16-2; the oxygen carrier in the oxidized state is conveyed to the gasification reactor 15 for circulation; the high-temperature oxygen-poor air and the air exchange heat in a second heat exchanger B11-2, the hot air is conveyed to the air regeneration reactor 18 and the carbon residue combustion reactor 17 to participate in the reaction, and the heat is recovered to reduce the energy loss;
the air regeneration reactor 18 is a fluidized bed, the regeneration reaction temperature is 1000-1100 ℃, and the fluidizing medium is hot air; the oxygen carrier and air regeneration reaction is a strong exothermic reaction, a spiral tube type heat exchanger is arranged outside the air regeneration reactor 18, part of reaction heat is removed and the temperature is regulated by introducing desalted water, and meanwhile, high-temperature steam is taken as a gasifying agent and is conveyed to the gasification reactor 15.
In an oxygen carrier air regeneration system, the following reactions mainly occur:
reduction of oxygen carrier particles
4Fe3O4+O2→6Fe2O3,ΔH298=-476kJ/mol。
In the technical scheme, the separation devices mainly comprise gas-solid separation and solid-solid separation, wherein the gas-solid separation device can be designed into a cyclone separator and a cyclone dust collector which are respectively used for gas-solid separation and flue gas dust removal; the solid-solid separation device can be designed as a boiling type magnetic separator (CN 204107645U) for CO2As transport media, magnetic Fe can be avoided3O4The particles are deeply oxidized, and simultaneously, the heat of the high-temperature solid is recycled, so that the magnetic separation effect can be optimized, the particles can be used as a gasification agent, and the energy utilization efficiency of the system is improved.
In the technical scheme, the pyrolysis reactor is designed as an internal heating fluidized bed reactor, and pyrolysis coal gas after heat exchange with high-temperature synthesis gas is used as a gas heat carrier to provide heat for the pyrolysis reaction; designing pyrolysis gas circulation amount, performing primary full circulation, and performing stable operation at 50% circulation amount; magnetic Fe3O4The oxygen carrier is used as a tar catalytic cracking catalyst, participates in pyrolysis reaction, and is circulated to an air regeneration reactor to remove tar cracking carbon deposition; oxygen carrier Fe3O4The temperature is designed to be 600-700 ℃ and is used as heat supplement for the pyrolysis reaction.
In the technical scheme, the gasification reactor is designed into a two-section type entrained flow reactor, the lower section is a lifting pipe, and the upper section is a cyclone type entrained flow bed; the riser not only leads the semicoke and the oxygen carrier Fe2O3The mixture is more uniform, and a rapid chemical chain gasification reaction is generated at the same time, so that the competitive reaction of a gasifying agent and an oxygen carrier in carbon reduction is reduced; the incision of the cyclone entrained flow bed is used for sample introduction, so that the gasifying agent is more fully contacted with the solid particles, and the reaction is more violent.
In the technical scheme, the regeneration reactor is designed into an internal combustion internal heating fluidized bed, and an externally wound spiral tube heat exchanger is designed to remove reaction heat in time so as to prevent the temperature runaway of the reactor; designing a supplementary gas burner, and maintaining the temperature of the reactor by using standby liquefied gas or pyrolysis gas (the pyrolysis gas can be used after being stored) as a heat source during the primary operation; when the reactor is stably operated, the temperature of the regeneration reactor is designed to be 1000-1100 ℃ depending on a large amount of reaction heat released by oxidation of the oxygen carrier, and the heat is conveyed to other units through the oxygen carrier.
The invention has the beneficial effects that: the invention realizes the double coupling of materials and energy among the coal pyrolysis unit, the coal coke chemical chain gasification unit and the oxygen carrier air regeneration unit. The invention couples the gas heat carrier coal pyrolysis technology, the tar catalytic cracking technology and the self-heating chemical chain gasification technology, the pyrolysis coal gas is used as the gas heat carrier for circulation, and the gasified synthetic gas is used as the heat source, thereby not only fully utilizing the waste heat of the gasification unit and realizing the high-efficiency utilization of energy, but also providing a hydrogen source for the light tar and strengthening the tar reforming effect. In addition, based on the principle of coal resource gradient conversion, carbon elements with different reaction activities in coal are utilized step by adopting different processes, so that the energy utilization efficiency of the system is improved.
Drawings
FIG. 1 is a schematic flow diagram of a system and a method for co-producing oil gas by coal gas cycle coal pyrolysis coupled chemical chain gasification.
FIG. 2 is a schematic diagram of material and energy distribution of the system and method for co-producing oil gas by coal gas cycle coal pyrolysis coupled chemical looping gasification.
In the figure: 1, a raw coal bin; 2 crushing and pulverizing device; 3, drying the reactor; 4-1 a first feed hopper a; 4-2 second feed hoppers B; 5-1 a first slide valve feeding device A; 5-2 second slide valve feeding device B; 6 a pyrolysis reactor; 7-1, a first cyclone dust collector A; 7-2 a second cyclone dust collector B; 8, a condenser; 9 an oil storage tank; 10-1 a first magnetic separation device A; 10-2 a second magnetic separation device B; 11-1 a first heat exchanger a; 11-2 second heat exchanger B; 12 gas-liquid separation tank; 13CO2An absorption tower; 14-1 a first fluidic device a; 14-2 second fluidic device B; 15 a gasification reactor; 16-1 a first cyclone a; 16-2 a second cyclone B; 16-3 a third cyclone separator C; 16-4 a fourth cyclone D; 17 a combustion reactor; 18 air regeneration reactor; 19 spiral tube heat exchanger; 20a mixer; 21 electric oil trap.
Detailed Description
The present invention will be described in further detail with reference to the following drawings and specific embodiments, but the present invention is not limited to the specific embodiments.
The system and the method for co-producing oil gas based on coal pyrolysis coupled chemical chain gasification in gas cycle are implemented by adopting the system, and the coal sample used in the following embodiment is Hessigla lignite, and the properties of the coal sample are shown in tables 1 and 2.
TABLE 1 Industrial and elemental analysis of raw coal
Note: is obtained by subtracting
TABLE 2 analysis of raw coal aluminum retort experiment
Example 1: in this example, the above-mentioned brown coal was used as a raw material, Fe2O3/Al2O3(73 wt%/27 wt%) as oxygen carrier. The specific operation process flow is shown in figure 1; the raw coal with the feeding amount of 100kg/h is crushed and sieved into fine powder with the particle size of 0.075mm, then the fine powder enters a drying reactor, the fine powder is mixed and dried with high-temperature flue gas at the temperature of 600 ℃ from a carbon residue combustion furnace and flue gas of a regeneration reactor after heat exchange, the temperature of the drying reactor is 120 ℃, at the temperature, a coal sample can be fully removed from the external water without pyrolysis reaction, and the dried coal sample enters the pyrolysis reactor. The water-containing flue gas is separated into waste water by a gas-liquid separation tank, and the waste water after sewage treatment can be used as a gasifying agent to be conveyed to a gasifying unit or used as condensed water in public works; flue gas passing through CO2An absorption tower for collecting carbon and using the residual heat of the carbon residue combustion furnace to carry out CO2Desorbing and separating CO2Can be used as a gasification agent or an inert carrier gas for transporting materials. Specific data are shown in table 3.
TABLE 3 drying Unit calculation results
The dried coal is mixed with an oxygen carrier (Fe/Al) from a gasification unit2O3) The particles are mixed and enter a pyrolysis reactor under the action of gravity to exchange heat with high-temperature coal gas at 700 ℃ from a heat exchanger, the temperature of the coal is raised to 500 ℃, pyrolysis reaction is carried out at the temperature, and pyrolysis coal gas (clean coal gas, tar gas and pyrolysis water) generated by pyrolysis enters a coal gas purification and tar recovery system after being dedusted by a high-efficiency cyclone dust collector. Pyrolyzing raw coal to generate high-temperature semicoke, and conveying the high-temperature semicoke to a gasification unit to participate in subsequent reaction; the generated pyrolysis coal gas and the high-temperature synthesis gas with the temperature of 900 ℃ from the gasification unit indirectly exchange heat in the heat exchanger and return to the pyrolysis reactor as a gas heat carrier. The temperature of the pyrolysis reactor is 500 ℃ and normal pressure. The pyrolysis products and energy distribution are shown in tables 4-8.
TABLE 4 conventional pyrolysis product distribution
TABLE 5 Industrial and elemental analysis of semicoke
TABLE 6 distillation range distribution of tar fractions
TABLE 7 pyrolysis gas composition distribution
TABLE 8 pyrolysis Unit calculation results
And the pyrolysis semicoke and the oxygen carrier generated by the pyrolysis reactor are separated by a magnetic separation device. The properties of the separated semicoke are shown in Table 5, and the high valence state oxygen carrier Fe at 1100 ℃ from the air regeneration unit2O3The particles are mixed and enter a gasification reactor, water vapor or pyrolysis gas is introduced to serve as a gasification agent, the water vapor serves as a fluidizing medium to enable gasification reaction to be rapidly generated, gas-solid separation of the synthetic gas and the oxygen carrier particles is achieved through a cyclone separator, the synthetic gas is stored as a product after heat is recovered through heat exchange, the low-valence oxygen carrier part serves as a solid heat carrier and a catalyst and returns to a pyrolysis unit, and the rest of the low-valence oxygen carrier part enters an air reactor for regeneration. Oxygen carrier Fe2O3The fixed carbon ratio in coal is 1 (mol ratio), the water vapor/fixed carbon ratio in coal is 0.6 (mol ratio), the temperature of the gasification reactor is 900 ℃, and the pressure is 20 atm. The gasification unit products are shown in tables 9-11.
TABLE 9 gas product distribution in gasification System
Gas component | H2 | CO | CH4 | CO2 | H2O | Others |
Volume fraction (%) | 32.31 | 47.64 | 8.43 | 9.46 | 1.2 | 0.96 |
TABLE 10 distribution of oxygen carrier valence states in gasification systems
TABLE 11 gasification Unit calculation results
The reduced oxygen carrier from the pyrolysis reactor and the gasification reactor enters an air regeneration reactor to perform oxidation regeneration reaction with air, and the oxygen carrier oxidized into a high-order oxidation state is conveyed to the gasification reactor to be circulated so as to provide lattice oxygen and heat required by chemical chain gasification reaction; the high-temperature oxygen-poor air exchanges heat with air, and the hot air is conveyed to the regeneration reactor and the carbon residue combustion reactor to participate in the reaction, wherein the temperature of the regeneration reactor is 1100 ℃ and 20 atm. The regeneration unit products are shown in tables 12-13.
TABLE 12 product distribution in the regeneration units
TABLE 13 reproduction Unit calculation results
The calculation results of each reaction unit are used for carrying out material and energy balance on the whole coupling system, and the results are shown in the attached figure 2. In addition, the energy loss of the single pyrolysis unit and the energy loss of the chemical chain unit are respectively 60.34kW and 150kW, the coupled system comprehensively considers the problem of waste heat recovery of products, the energy loss is only 35.22kW, the utilization efficiency of system energy is obviously improved, the investment of coke quenching and synthetic gas cooling equipment is avoided, and certain equipment cost is reduced.
Claims (8)
1. A system for co-producing oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification is characterized by comprising a raw coal pretreatment system, a coal pyrolysis system, a coal coke chemical chain gasification system and an oxygen carrier air regeneration system;
a raw coal pretreatment system comprises a raw coal bunker (1), a crushing and pulverizing device (2), a drying reactor (3), a gas-liquid separation tank (12) and CO2An absorption tower (13); raw coal in a raw coal bin (1) is made into pulverized coal with the particle size of 0.05-0.1 mm through a crushing powder-making device (2), and the pulverized coal and high-temperature dust-removing flue gas generated by a carbon residue combustion reactor (17) in a coke chemical chain gasification system are mixed, dried and pretreated in a drying reactor (3); the waste water of the water-containing waste gas generated in the drying reactor (3) is separated by a gas-liquid separation tank (12) and then passes through CO2CO separation in an absorption column (13)2And N2Taking the dried coal sample as a raw material to enter a coal pyrolysis system;
the coal pyrolysis system comprises a feeding hopper, a slide valve feeding device, a pyrolysis reactor (6), a two-stage cyclone separator (22), a first cyclone dust collector A (7-1), a condenser (8), an oil storage tank (9), an electric oil catcher (21), a first magnetic separation device A (10-1) and a first heat exchanger A (11-1); raw coal pretreated by the drying reactor (3) sequentially passes through a first feeding hopper A (4-1) and a first slide valve feeding device A (5-1), and a reduced oxygen carrier sequentially passes through a first feeding hopper B (4-2) and a second slide valve feeding device B (5-2) to enter a pyrolysis reactor (6) with a two-stage cyclone separator (22) arranged inside, and semicoke, tar and pyrolysis coal gas are obtained in the pyrolysis reactor (6); pyrolysis gas and tar mixture enter a first cyclone dust collector A (7-1) from the upper outlet end of a pyrolysis reactor (6), and after dust removal treatment of the first cyclone dust collector A (7-1), tar enters a condenser (8), is condensed by the condenser (8), and is stored in an oil storage tank (9); an electric oil catcher (21) is arranged at the outlet of the oil storage tank (9) and is used for recovering tar carried by gas; the pyrolysis coal gas after tar recovery and the high-temperature gasification synthesis gas generated by the coal coke chemical-looping gasification system exchange heat in a first heat exchanger A (11-1) and then enter a pyrolysis reactor (6) as a gas heat carrier; the semicoke and the reduced-state oxygen carrier enter a first magnetic separation device A (10-1) through the lower outlet end of a pyrolysis reactor (6), are separated by the first magnetic separation device A (10-1), the semicoke is used as a raw material of a coal coke chemical-looping gasification system, and the reduced-state oxygen carrier is regenerated in an air regeneration reactor (18);
the coal coke chemical chain gasification system comprises a jet device, a gasification reactor (15), a first cyclone separator A (16-1), a second magnetic separation device B (10-2), a carbon residue combustion reactor (17) and a second cyclone dust collector B (7-2); the semicoke fed by the first jet device A (14-1) and the oxidation state oxygen carrier fed by the second jet device B (14-2) enter a gasification reactor (15) together, and a gasification agent CO is supplemented2And H2O, carrying out gasification reaction to prepare synthesis gas; the gasification product enters a first cyclone separator A (16-1) from an outlet at the top end of the gasification reactor (15), and the synthesis gas and the solid phase residue are separated by the first cyclone separator A (16-1); exchanging heat between the high-temperature synthesis gas and low-temperature pyrolysis gas generated by a coal pyrolysis system in a first heat exchanger A (11-1), and taking the synthesis gas with recovered heat as a product to be stored in a tank area; separating a reduced oxygen carrier and unreacted carbon from the solid-phase residue by a second magnetic separation device B (10-2), fully combusting the unreacted carbon in a combustion reactor (17) to generate high-temperature flue gas, and dedusting the dusty flue gas in a second cyclone dust collector B (7-2) and then feeding the dedusted flue gas into a drying reactor (3) to provide heat for drying raw coal; the reduced oxygen carrier is partially returned to the pyrolysis reactor (6)) As a solid heat carrier and a catalyst, oxidizing the rest of reduced oxygen carriers into high-valence oxygen carriers in an air regeneration reactor (18);
the oxygen carrier air regeneration system comprises a mixer (20), an air regeneration reactor (18), a spiral tube type heat exchanger (19), a second cyclone separator B (16-2) and a second heat exchanger B (11-2); the reduced oxygen carrier of the coal pyrolysis system and the coal coke chemical looping gasification system enters an air regeneration reactor (18) with an external spiral tube type heat exchanger (19) together with hot air through a mixer (20) to carry out oxidation regeneration reaction, so as to obtain a high-order oxidation state oxygen carrier and oxygen-deficient air; the oxygen carrier in the oxidation state and the oxygen-deficient air are separated in a second cyclone separator B (16-2); the oxygen carrier in an oxidized state is conveyed to the gasification reactor (15) for circulation; the high-temperature oxygen-poor air and air exchange heat in a second heat exchanger B (11-2), and hot air is conveyed to an air regeneration reactor (18) and a carbon residue combustion reactor (17) to participate in the reaction, so that heat is recovered, and energy loss is reduced.
2. The system for co-production of oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification as claimed in claim 1, wherein the pyrolysis reactor (6) is an internal heating fluidized bed reactor, the reaction is divided into an upper section and a lower section, the lower section is a dense phase region, the upper section is a dilute phase region, a two-stage cyclone separator (22) is arranged in the pyrolysis reactor, and the lower end of the cyclone separator (22) is provided with a wing valve; the temperature of the pyrolysis reactor (6) is 500-600 ℃, and the oxygen carrier from the gasification reactor is Fe3O4The catalytic cracking of tar is promoted by the continuous release and supplement of lattice oxygen; after external heat exchange, the pyrolysis gas at 650-750 ℃ is used as a gas heat carrier and returns to the pyrolysis reactor (6) to provide heat for the pyrolysis reaction; the 550-650 ℃ reduced oxygen carrier with catalytic action enters the pyrolysis reactor (6) through a second slide valve feeding device B (5-2) and the coal sample at the same time; the temperature of the condenser (8) is 120-150 ℃, the quality of tar is improved, and meanwhile, phenol-containing wastewater provides a hydrogen source for the lightening of the tar.
3. The coal gas cycle coal pyrolysis coupled chemical looping gasification co-production of oil gas according to claim 1 or 2The system is characterized in that the gasification reactor (15) is a vertical cyclone furnace, the temperature of the gasification reactor (15) is 800-900 ℃, and the temperature of Fe from the air regeneration reactor (18) is 1000-1100 DEG C2O3The oxygen carrier is used as a solid heat carrier to provide heat for gasification reaction; a two-section type gasification reactor (15), the lower section is a fast reaction section for direct chemical chain gasification of coal coke and oxygen carrier, and the upper section is a hydrogen production reaction of Fe/FeO and steam, so as to realize H in synthesis gas2the/CO is adjustable; the gasification reactor (15) is fed in a manner of opposed feeding such that the semicoke and Fe are2O3The mixing is more uniform, and the collision reaction is more violent; the carbon content of ash is 6-10%, the temperature of a carbon residue combustion reactor is 500-600 ℃, and the step conversion and comprehensive utilization of coal are realized through high-temperature flue gas heat exchange.
4. The system for co-production of oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification as claimed in claim 1 or 2, wherein the air regeneration reactor (18) is a fluidized bed, the regeneration reaction temperature is 1000-1100 ℃, and the fluidizing medium is hot air; the oxygen carrier and air regeneration reaction is strong exothermic reaction, a spiral tube type heat exchanger is arranged outside the air regeneration reactor (18), partial reaction heat is removed and the temperature is regulated by introducing desalted water, and meanwhile, high-temperature steam is taken as a gasifying agent and is conveyed to the gasification reactor (15).
5. The system for co-production of oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification as claimed in claim 3, wherein the air regeneration reactor (18) is a fluidized bed, the regeneration reaction temperature is 1000-1100 ℃, and the fluidizing medium is hot air; the oxygen carrier and air regeneration reaction is strong exothermic reaction, a spiral tube type heat exchanger is arranged outside the air regeneration reactor (18), partial reaction heat is removed and the temperature is regulated by introducing desalted water, and meanwhile, high-temperature steam is taken as a gasifying agent and is conveyed to the gasification reactor (15).
6. The system for co-production of oil gas by coal gas circulation, coal pyrolysis and chemical chain gasification according to claim 1, 2 or 5, wherein the separation device mainly comprises gas-solid separation and solid-solid separation, the gas-solid separation device comprises a cyclone separator and a cyclone dust collector, and the separation efficiency is 95-99%; the solid-solid separation adopts a magnetic separation mode, and the separation efficiency is 95-99%.
7. The system for co-production of oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification as claimed in claim 3, wherein the separation device mainly comprises gas-solid separation and solid-solid separation, wherein the gas-solid separation device comprises a cyclone separator and a cyclone dust collector, and the separation efficiency is 95-99%; the solid-solid separation adopts a magnetic separation mode, and the separation efficiency is 95-99%.
8. The system for co-production of oil gas by coal gas circulation coal pyrolysis coupling chemical chain gasification as claimed in claim 4, wherein the separation device mainly comprises gas-solid separation and solid-solid separation, wherein the gas-solid separation device comprises a cyclone separator and a cyclone dust collector, and the separation efficiency is 95-99%; the solid-solid separation adopts a magnetic separation mode, and the separation efficiency is 95-99%.
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